A short tandem repeat-based phylogeny for the human Y chromosome

被引:113
作者
Forster, P
Röhl, A
Lünnemann, P
Brinkmann, C
Zerjal, T
Tyler-Smith, C
Brinkmann, B
机构
[1] Univ Munster, Inst Rechtsmed, D-48149 Munster, Germany
[2] Univ Cambridge, McDonald Inst Archaeol Res, Cambridge, England
[3] Univ Oxford, Dept Biochem, Oxford OX1 3QU, England
基金
英国惠康基金;
关键词
D O I
10.1086/302953
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Human Y-chromosomal short tandem repeat (STR) data provide a potential model system for the understanding of autosomal STR mutations in humans and other species. Yet, the reconstruction of STR evolution is rarely attempted, because of the absence of an appropriate methodology We here develop and validate a phylogenetic network approach. We have typed 256 Y chromosomes of indigenous descent from Africa, Asia, Europe, Australia, and highland Papua Near Guinea, for the STR loci DYS19, DXYS156Y, DYS389, DYS390, DYS392, and DYS393, as well as for five ancient biallelic mutation events: two poly (A) length variants associated with the YAP insertion, two independent SRY-1532 mutations, and the 92R7 mutation. We have used our previously published pedigree data from 11,000 paternity-tested autosomal STR-allele transfers to produce a two-class weighting system for the Y-STR loci that is based on locus lengths and motif lengths. Reduced-median-network analysis yields a phylogeny that is independently supported by the five biallelic mutations, with an error of 6%. We find the earliest branch in our African San (Bushmen) sample. Assuming an age of 20,000 years for the Native American DYS199 T mutation, we estimate a mutation rate of 2.6 x 10(-4) mutations/20 years for slowly mutating Y STRs, similar to 10-fold slower than the published average pedigree rate.
引用
收藏
页码:182 / 196
页数:15
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